Canonical Allele Identifier: CA919611511
Gene:

Linked Data

dbSNP Id: rs1567075155

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419506del , CM000677.2:g.87419506del GRCh38
NC_000015.9:g.87962737del , CM000677.1:g.87962737del GRCh37
NC_000015.8:g.85763741del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932584.1:n.339+225del
XR_932585.1:n.339+225del
XR_001751647.1:n.616+225del
XR_932585.2:n.626+225del